# Passy-Muir, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/passy-muir-inc/7c161136-6f09-4f6f-94a7-828a6da424ae

> Inspection records and compliance data for Passy-Muir, Inc. in Irvine, California. Access full analysis and detailed observations.

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## Details

- Name: Passy-Muir, Inc.
- FEI Number: 2024841
- City: Irvine
- State: California
- Country Name: United States
- Address Line 1: 17992 Mitchell S Ste 200
- Zip Code: 92614

## Related Documents

- [FDA Inspection 1255752 - Passy-Muir, Inc. - 2024-11-01](https://www.keypedia.com/records/fda_inspections/passy-muir-inc/f04b95b0-c707-45aa-88b0-e2c7652b4369) — source: FDA, date: November 1, 2024
- [FDA Inspection 1255752 - Passy-Muir, Inc. - 2024-11-01](https://www.keypedia.com/records/fda_inspections/passy-muir-inc/bd31a2e8-c156-4d2b-9f5d-9e7125aa6579) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2024
- [FDA Inspection 1255752 - Passy-Muir, Inc. - 2024-11-01](https://www.keypedia.com/records/fda_inspections/passy-muir-inc/b481ba15-4c16-4573-bcbd-d133bf970673) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2024
- [FDA Inspection 1069141 - Passy-Muir, Inc. - 2018-08-30](https://www.keypedia.com/records/fda_inspections/passy-muir-inc/71b675c1-6087-4fc6-8acd-f2479e6caf96) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2018
- [FDA Inspection 1069141 - Passy-Muir, Inc. - 2018-08-30](https://www.keypedia.com/records/fda_inspections/passy-muir-inc/d8a41885-16d2-4591-90ee-9cae8f23d192) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2018
- [FDA Inspection 786168 - Passy-Muir, Inc. - 2012-05-19](https://www.keypedia.com/records/fda_inspections/passy-muir-inc/9eae7b75-90c3-4caa-b601-fcda0f12095e) — classification: No Action Indicated (NAI), source: FDA, date: May 19, 2012
- [FDA Inspection 786168 - Passy-Muir, Inc. - 2012-05-19](https://www.keypedia.com/records/fda_inspections/passy-muir-inc/b7af6808-02b2-4d09-ae3b-e5e0c01af4dd) — classification: No Action Indicated (NAI), source: FDA, date: May 19, 2012

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